Wolff B G, Bolton J, Baum R, Chetanneau A, Pecking A, Serafini A N, Fischman A J, Hoover H C, Klein J L, Wynant G E, Subramanian R, Goroff D K, Hanna M G
Department of Colorectal and General Surgery, Mayo Clinic, Rochester, Minnesota, USA.
Dis Colon Rectum. 1998 Aug;41(8):953-62. doi: 10.1007/BF02237380.
The study contained herein was undertaken to evaluate the accuracy of radiolabeled human monoclonal antibody, 88BV59H21-2V67-66 (88BV59 or HumaSPECT-Tc), in predicting disease resectability in presurgical subjects with recurrent, metastatic, or occult colorectal carcinoma.
A total of 219 patients with disease visualized on computed tomographic scan (recurrent or metastatic disease) or with negative or equivocal computed tomographic scan and rising carcinoembryonic antigen serum levels (occult group) received technetium Tc99m-labeled 88BV59 intravenously. Planar and single photon emission computed tomograhic images were obtained 14 to 20 hours postinfusion, before surgery. The ability of computed tomographic and HumaSPECT-Tc imaging to define the extent of disease and to predict resectability was evaluated based on surgical and histopathologic results.
In patients with recurrent or metastatic disease (170 evaluable patients), the accuracy of predicting nonresectability of disease was significantly greater (P < 0.001) for HumaSPECT-Tc than for computed tomography (60 vs 29 percent). Computed tomography understaged 41 percent of patients believed to have resectable disease compared with 27 percent for HumaSPECT-Tc (P < 0.001). In occult disease patients (29 computed tomographic and 28 HumaSPECT-Tc evaluable patients), the overall accuracy of predicting resectability/nonresectability was 6 percent for HumaSPECT-Tc compared with 24 percent from computed tomography. Administration of HumaSPECT-Tc had no effect on monoclonal antibody-based in vitro diagnostic assays. Only a single patient demonstrated an anti-antibody response (90 ng/ml) at nine weeks postinfusion.
HumaSPECT-Tc was more accurate than computed tomography in determining disease resectability in patients with metastatic, recurrent, or occult cancer. The addition of HumaSPECT-Tc imaging can play a significant role in patient management decisions.
开展本研究以评估放射性标记的人单克隆抗体88BV59H21 - 2V67 - 66(88BV59或HumaSPECT - Tc)在预测复发性、转移性或隐匿性结直肠癌术前患者疾病可切除性方面的准确性。
共有219例患者,其疾病在计算机断层扫描(CT)上可见(复发性或转移性疾病),或CT扫描阴性或结果不明确且癌胚抗原血清水平升高(隐匿组),静脉注射锝Tc99m标记的88BV59。在输液后14至20小时、手术前获取平面和单光子发射计算机断层扫描图像。基于手术和组织病理学结果,评估CT和HumaSPECT - Tc成像确定疾病范围和预测可切除性的能力。
在复发性或转移性疾病患者(170例可评估患者)中,HumaSPECT - Tc预测疾病不可切除性的准确性显著高于CT(P < 0.001)(分别为60%和29%)。与HumaSPECT - Tc的27%相比,CT对41%被认为有可切除疾病的患者分期过低(P < 0.001)。在隐匿性疾病患者(29例CT可评估患者和28例HumaSPECT - Tc可评估患者)中,HumaSPECT - Tc预测可切除性/不可切除性的总体准确性为6%,而CT为24%。HumaSPECT - Tc的给药对基于单克隆抗体的体外诊断测定无影响。仅1例患者在输液后9周出现抗抗体反应(90 ng/ml)。
在确定转移性、复发性或隐匿性癌症患者的疾病可切除性方面,HumaSPECT - Tc比CT更准确。添加HumaSPECT - Tc成像可在患者管理决策中发挥重要作用。